Responsible for general activity, off line and on line packing activity in parenteral packing. • Clearance of packing area. • Process of secondary packing. • Verification of packing materials. • Weighing balance and its verification. • Veri...

"TBD"...

"TBD"...

Responsible for general activity, off line and on line packing activity in parenteral packing. • Clearance of packing area. • Process of secondary packing. • Verification of packing materials. • Weighing balance and its verification. • Veri...

To plan daily packing activity per norms of cGMP. • To carryout dry cleanig and packing activity as per requirement in Cephalosporin block. • To optimize utilization of Machines. • To carry out in process checks during packing activities. •...

Ensure the development progress periodically of personals and take necessary corrective action. • Ensure the compliance of inspection /Audit in coating area and revision of procedures/SOPs • To follow daily plan prepared based on the monthl...

"• Ensure efficient operation and maintenance of Utility (Boiler, chilling plant, Air compressor, cooling tower and N2 System). • To ensure strict compliance of cGMP requirements & Good Engineering Practice requirements besides other statut...

"To perform the in process checks for control on production for the process / product being manufactured. To ensure Quality and cGMP compliance of the products being manufactured. Parenteral Manufacturing : • To give Area /Equipment clearan...

To plan daily packing activity per norms of cGMP. • To carryout dry cleanig and packing activity as per requirement in Cephalosporin block. • To optimize utilization Machines. • To ensure that all records / documents for compliance to regul...

Ensure receipt and on-line documentation of the materials received as per SOP. • Ensure all the operating systems are maintained as per the SOP. • To receive the materials as per the amended approved vendor list. • To store materials as per...

"• Responsible for small volume parenteral manufacturing activities at Dholka premises. • To check hygienic condition of the workmen before entering to aseptic area, processing area and compounding area and maintain record. • To check and e...

To check and ensure that differential pressure of the working area are within limit and record it properly. • To check and ensure that differential pressure of all Laminar Air Flow are within limit and record it properly. • To check on line...

Receipt of Raw Material for main Pharma stores. • SAP data entries like GRN, Issuance, Transfer posting, reservations, SAP report generation etc. • To check the environmental parameters like Temperature, RH, pressure difference etc. • Daily...

"To supervise the Manufacturing & Packing Line Activities with compliance of cGMP and Regulatory requirements to ensure timely completion of the work. Setting daily/weekly/monthly objectives and communicating them to employees Organizing wo...

Major purpose of the job : • Responsible for overall management of Biotech-QC department. Principal task and responsibilities : • Ensuring planning of the QC functional activities and sample analysis execution activity completed on time to ...

To meet agreed production targets with due compliance to regulatory norms. • To ensure proper utilization and productivity of manpower and machines. • To ensure all records/documents of department are maintained in compliance to regulatory....

Responsible for small volume parenteral manufacturing activities at Dholka premises. • To check hygienic condition of the workmen before entering to aseptic area, processing area and compounding area and maintain record. • To check and ensu...

"• To operate Water system RO1, RO2, RO3, RO5 plant as per SOP at Dholka. • To carry out Preventive maintenance of Water system equipment’s. • Treatment of Water to be done in Water system as per SOP. • Records to be update as per cGMP norm...

Management of stores activities for Raw and Packing materials. Storage, Dispensing & Dispatches of Raw materials in Cephalosporin Stores. Training to the Staff / workmen at their area of works as per SOP. To ensure Quality and cGMP complian...

Follow cGMP and GLP practices in Quality Control Lab. • To analyze the Sample of raw material on non-chromatographic instrument such as FTIR, UV, Polarimeter, KF, Autotitrator etc. by following test procedure. • To attend the training as pe...